A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443226



Internal ID21100779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57627619..57627735hg38UCSC Ensembl
chr10:59387379..59387495hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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